Primary Site >> Stomach Cancer

Gene >> S1PR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305352
Start 101239862:101239862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.878C>T
AA Mutation p.Ala293Val(p.A293V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305352
Start 101239444:101239444(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.460G>A
AA Mutation p.Gly154Arg(p.G154R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305352
Start 101239099:101239099(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140298731
CDS Mutation c.115G>A
AA Mutation p.Ala39Thr(p.A39T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000305352
Start 101240048:101240048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1064C>T
AA Mutation p.Ser355Leu(p.S355L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000305352
Start 101239468:101239468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.484C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000305352
Start 101239755:101239755(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771C>T
Mutation Classification Silent
Feature Type Transcript